PE20081496A1 - Derivados de 2,5-dihidro-3-h-pirazolo[4,3-c]piridazin-3-ona sustituidos como antagonistas de los receptores cb1 - Google Patents
Derivados de 2,5-dihidro-3-h-pirazolo[4,3-c]piridazin-3-ona sustituidos como antagonistas de los receptores cb1Info
- Publication number
- PE20081496A1 PE20081496A1 PE2007001610A PE2007001610A PE20081496A1 PE 20081496 A1 PE20081496 A1 PE 20081496A1 PE 2007001610 A PE2007001610 A PE 2007001610A PE 2007001610 A PE2007001610 A PE 2007001610A PE 20081496 A1 PE20081496 A1 PE 20081496A1
- Authority
- PE
- Peru
- Prior art keywords
- phenyl
- ona
- pirazolo
- dihidro
- receptors
- Prior art date
Links
- 239000005557 antagonist Substances 0.000 title 1
- -1 PYRROLYL Chemical class 0.000 abstract 3
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical class [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 abstract 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical class [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 abstract 2
- SCVJRXQHFJXZFZ-KVQBGUIXSA-N 2-amino-9-[(2r,4s,5r)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-3h-purine-6-thione Chemical compound C1=2NC(N)=NC(=S)C=2N=CN1[C@H]1C[C@H](O)[C@@H](CO)O1 SCVJRXQHFJXZFZ-KVQBGUIXSA-N 0.000 abstract 1
- SLRMQYXOBQWXCR-UHFFFAOYSA-N 2154-56-5 Chemical compound [CH2]C1=CC=CC=C1 SLRMQYXOBQWXCR-UHFFFAOYSA-N 0.000 abstract 1
- WZKSXHQDXQKIQJ-UHFFFAOYSA-N F[C](F)F Chemical class F[C](F)F WZKSXHQDXQKIQJ-UHFFFAOYSA-N 0.000 abstract 1
- 229930003827 cannabinoid Natural products 0.000 abstract 1
- 239000003557 cannabinoid Substances 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- QUPDWYMUPZLYJZ-UHFFFAOYSA-N ethyl Chemical compound C[CH2] QUPDWYMUPZLYJZ-UHFFFAOYSA-N 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 208000015122 neurodegenerative disease Diseases 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 239000000825 pharmaceutical preparation Substances 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
- 208000020016 psychiatric disease Diseases 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D231/18—One oxygen or sulfur atom
- C07D231/20—One oxygen atom attached in position 3 or 5
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/5025—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring systems
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
- C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
- C07D237/06—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D285/00—Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
- C07D285/01—Five-membered rings
- C07D285/02—Thiadiazoles; Hydrogenated thiadiazoles
- C07D285/04—Thiadiazoles; Hydrogenated thiadiazoles not condensed with other rings
- C07D285/06—1,2,3-Thiadiazoles; Hydrogenated 1,2,3-thiadiazoles
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/06—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Diabetes (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Addiction (AREA)
- Hospice & Palliative Care (AREA)
- Rheumatology (AREA)
- Immunology (AREA)
- Child & Adolescent Psychology (AREA)
- Physical Education & Sports Medicine (AREA)
- Psychology (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Emergency Medicine (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Endocrinology (AREA)
- Otolaryngology (AREA)
- Anesthesiology (AREA)
- Gastroenterology & Hepatology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
SE REFIERE A DERIVADOS DE 2,5-DIHIDRO-3-H-PIRAZOLO[4,3-C]PIRIDAZIN-3-ONA SUSTITUIDOS DE FORMULA (I), EN DONDE R1 ES UN ALQUILO(C1-C12), CARBOCICLO NO AROMATICO(C3-C12), FENILO, PIRROLILO, ENTRE OTROS; R2 Y R3 SON INDEPENDIENTEMENTE FENILO SUSTITUIDO O NO POR HALOGENO, HIDROXI, -O(CH2)mR5, ENTRE OTROS; R4 ES H, ALQUILO(C1-C4), ALCOXI(C1-C4) O HIDROXI; R5 ES -NR7R8 O -SAlk. SON SELECCIONADOS: 5-(4-CLOROFENIL)-6-(2,4-DICLOROFENIL)-2-(4-ISOPROPILBENCIL)-2,5-DIHIDRO-3H-PIRAZOLO[4,3-c]PIRIDAZIN-3-ONA, N-{2-[(3-CLORO-4-{5-[4-(METILTIO)FENIL]-3-OXO-2-[4-(TRIFLUORO-METIL)BENCIL]-3,5-DIHIDRO-2H-PIRAZOLO[4,3-c]PIRIDAZIN-6-IL}FENIL)TIO]ETIL}CICLO-PROPANOCARBOXAMIDA, ENTRE OTROS. SE REFIERE TAMBIEN A UN PROCEDIMIENTO DE PREPARACION Y COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON UTILES EN EL TRATAMIENTO O PREVENCION DE ENFERMEDADES LIGADAS A LOS RECEPTORES DE CANNABINOIDES CB1, TALES COMO TRASTORNOS DE PSIQUIATRICOS Y/O NEURODEGENERATIVOS
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0610371A FR2909090B1 (fr) | 2006-11-23 | 2006-11-23 | Derives de 2,5-dihydro-3h-pyrazolo[4,3-c]pyridazin-3-one substitues,leur preparation et leur application en therapeutique. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20081496A1 true PE20081496A1 (es) | 2009-01-04 |
Family
ID=38229329
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2007001610A PE20081496A1 (es) | 2006-11-23 | 2007-11-20 | Derivados de 2,5-dihidro-3-h-pirazolo[4,3-c]piridazin-3-ona sustituidos como antagonistas de los receptores cb1 |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US7915258B2 (es) |
| EP (1) | EP2094706B1 (es) |
| JP (1) | JP2010510297A (es) |
| KR (1) | KR20090092774A (es) |
| CN (1) | CN101541802A (es) |
| AR (1) | AR063898A1 (es) |
| AT (1) | ATE494290T1 (es) |
| AU (1) | AU2007330652A1 (es) |
| BR (1) | BRPI0719291A2 (es) |
| CA (1) | CA2668196A1 (es) |
| CL (1) | CL2007003346A1 (es) |
| DE (1) | DE602007011815D1 (es) |
| FR (1) | FR2909090B1 (es) |
| IL (1) | IL198523A0 (es) |
| MX (1) | MX2009005447A (es) |
| PE (1) | PE20081496A1 (es) |
| RU (1) | RU2009123841A (es) |
| TW (1) | TW200836739A (es) |
| UY (1) | UY30742A1 (es) |
| WO (1) | WO2008068424A2 (es) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW200920372A (en) * | 2007-07-13 | 2009-05-16 | Genelabs Tech Inc | Anti-viral compounds, compositions, and methods of use |
| US8293744B2 (en) | 2009-04-20 | 2012-10-23 | Merck Sharp & Dohme Corp. | Heterocyclic fused cinnoline M1 receptor positive allosteric modulators |
| JP5800813B2 (ja) * | 2010-08-04 | 2015-10-28 | 武田薬品工業株式会社 | 複素環化合物 |
| TW201400446A (zh) | 2012-05-22 | 2014-01-01 | Genentech Inc | N-取代之苯甲醯胺及其使用方法 |
| WO2015038655A1 (en) | 2013-09-12 | 2015-03-19 | Alios Biopharma, Inc. | Aza-pyridone compounds and uses thereof |
| MX370085B (es) * | 2013-09-12 | 2019-11-29 | Janssen Biopharma Inc | Compuestos de piridazinona y usos de los mismos. |
| JP6422164B2 (ja) | 2013-12-26 | 2018-11-14 | 塩野義製薬株式会社 | 含窒素6員環誘導体およびそれらを含有する医薬組成物 |
| CN107531717B (zh) | 2015-03-11 | 2021-07-27 | 詹森生物制药有限公司 | 氮杂-吡啶酮化合物及其用途 |
| TWI715569B (zh) | 2015-04-24 | 2021-01-11 | 日商塩野義製藥股份有限公司 | 6員雜環衍生物及含有彼等之醫藥組合物 |
| US11066409B2 (en) | 2016-10-17 | 2021-07-20 | Shionogi & Co., Ltd. | Bicyclic nitrogen-containing heterocyclic derivatives and pharmaceutical composition comprising the same |
| PH12022550597A1 (en) | 2019-09-16 | 2024-03-04 | Takeda Pharmaceuticals Co | Azole-fused pyridazin-3(2h)-one derivatives |
| TW202321229A (zh) | 2021-08-18 | 2023-06-01 | 美商富曼西公司 | 殺真菌的取代的雜環化合物 |
| CN118546389B (zh) * | 2024-07-29 | 2024-10-15 | 陕西理工大学 | 哒嗪氢键骨架荧光传感材料及其制备方法和应用 |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4345934A (en) | 1977-03-10 | 1982-08-24 | Rohm And Haas Company | Method of producing hybrid cereal grain seeds by application of 1-aryl-1,4-dihydro-4-oxo(thio)-pyridazines |
| FR2692575B1 (fr) | 1992-06-23 | 1995-06-30 | Sanofi Elf | Nouveaux derives du pyrazole, procede pour leur preparation et compositions pharmaceutiques les contenant. |
| FR2713225B1 (fr) | 1993-12-02 | 1996-03-01 | Sanofi Sa | N-pipéridino-3-pyrazolecarboxamide substitué. |
| US6005103A (en) | 1993-11-19 | 1999-12-21 | Warner-Lambert Company | Pyrone derivatives as protease inhibitors and antiviral agents |
| US5808082A (en) * | 1996-05-08 | 1998-09-15 | Merck & Co., Inc. | Method of preparing phosphodiesterase IV inhibitors |
| FR2789079B3 (fr) | 1999-02-01 | 2001-03-02 | Sanofi Synthelabo | Derive d'acide pyrazolecarboxylique, sa preparation, les compositions pharmaceutiques en contenant |
| US7601718B2 (en) * | 2003-02-06 | 2009-10-13 | Vertex Pharmaceuticals Incorporated | Compositions useful as inhibitors of protein kinases |
| US7232823B2 (en) * | 2003-06-09 | 2007-06-19 | Pfizer, Inc. | Cannabinoid receptor ligands and uses thereof |
| WO2005061504A1 (en) * | 2003-12-16 | 2005-07-07 | Pfizer Products Inc. | Bicyclic pyridazinone cannabinoid receptor ligands and uses thereof |
| US8299257B2 (en) * | 2007-09-20 | 2012-10-30 | Glaxo Group Limited | Compounds which have activity at M1receptor and their uses in medicine |
-
2006
- 2006-11-23 FR FR0610371A patent/FR2909090B1/fr not_active Expired - Fee Related
-
2007
- 2007-11-19 KR KR1020097010476A patent/KR20090092774A/ko not_active Withdrawn
- 2007-11-19 JP JP2009537670A patent/JP2010510297A/ja not_active Withdrawn
- 2007-11-19 CA CA002668196A patent/CA2668196A1/fr not_active Abandoned
- 2007-11-19 RU RU2009123841/04A patent/RU2009123841A/ru not_active Application Discontinuation
- 2007-11-19 CN CNA2007800431890A patent/CN101541802A/zh active Pending
- 2007-11-19 BR BRPI0719291-6A patent/BRPI0719291A2/pt not_active Application Discontinuation
- 2007-11-19 WO PCT/FR2007/001889 patent/WO2008068424A2/fr not_active Ceased
- 2007-11-19 MX MX2009005447A patent/MX2009005447A/es not_active Application Discontinuation
- 2007-11-19 EP EP07870295A patent/EP2094706B1/fr active Active
- 2007-11-19 AU AU2007330652A patent/AU2007330652A1/en not_active Abandoned
- 2007-11-19 AT AT07870295T patent/ATE494290T1/de not_active IP Right Cessation
- 2007-11-19 DE DE602007011815T patent/DE602007011815D1/de active Active
- 2007-11-20 TW TW096143951A patent/TW200836739A/zh unknown
- 2007-11-20 PE PE2007001610A patent/PE20081496A1/es not_active Application Discontinuation
- 2007-11-22 AR ARP070105186A patent/AR063898A1/es unknown
- 2007-11-22 CL CL200703346A patent/CL2007003346A1/es unknown
- 2007-11-23 UY UY30742A patent/UY30742A1/es not_active Application Discontinuation
-
2009
- 2009-05-03 IL IL198523A patent/IL198523A0/en unknown
- 2009-05-19 US US12/468,294 patent/US7915258B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| WO2008068424A2 (fr) | 2008-06-12 |
| KR20090092774A (ko) | 2009-09-01 |
| CA2668196A1 (fr) | 2008-06-12 |
| FR2909090A1 (fr) | 2008-05-30 |
| JP2010510297A (ja) | 2010-04-02 |
| FR2909090B1 (fr) | 2009-01-09 |
| EP2094706A2 (fr) | 2009-09-02 |
| MX2009005447A (es) | 2009-08-07 |
| WO2008068424A3 (fr) | 2008-07-24 |
| CL2007003346A1 (es) | 2008-07-04 |
| AU2007330652A1 (en) | 2008-06-12 |
| US20090281107A1 (en) | 2009-11-12 |
| EP2094706B1 (fr) | 2011-01-05 |
| IL198523A0 (en) | 2010-02-17 |
| BRPI0719291A2 (pt) | 2014-02-25 |
| UY30742A1 (es) | 2008-07-03 |
| US7915258B2 (en) | 2011-03-29 |
| ATE494290T1 (de) | 2011-01-15 |
| AR063898A1 (es) | 2009-02-25 |
| WO2008068424A8 (fr) | 2009-07-02 |
| TW200836739A (en) | 2008-09-16 |
| CN101541802A (zh) | 2009-09-23 |
| DE602007011815D1 (de) | 2011-02-17 |
| RU2009123841A (ru) | 2010-12-27 |
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